Remote Oncology AI Research Evaluator

Alignerr Corp.

Dallas (TX)

Remote

USD 83,000 - 165,000

Part time

5 days ago
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Benefits offered by this job

Fully remote
Flexible schedule
Freelance autonomy
Contract extension potential
Collaboration with leading AI teams

Job summary

Alignerr is seeking an experienced Oncology Clinical Researcher to shape how AI understands oncology by grounding models in real-world clinical trial science. You will review and improve AI-generated oncology content, ensuring regulatory-aligned, scientifically valid outputs.

You’ll work remotely on an hourly contract, 10–40 hours per week, with flexible scheduling. This role suits professionals who want meaningful, independent work and potential ongoing projects with leading AI research teams.

Qualifications

  • Experience designing and managing oncology trials from protocol development through data readout.
  • Ability to assess endpoints, safety, and biomarkers in oncology data.
  • Familiar with FDA/EMA submission standards and regulatory compliance.

Responsibilities

  • Review AI-generated oncology content for clinical accuracy, scientific validity, and regulatory alignment.
  • Assess study protocols, patient enrollment logic, and compliance with ethical and regulatory standards.
  • Analyze AI outputs related to cancer trial data — including safety profiles, efficacy endpoints, and biomarker findings.
  • Evaluate AI-generated regulatory and scientific reporting against FDA/EMA submission standards.
  • Provide structured, expert feedback that directly improves how frontier AI systems reason about oncology.
  • Work independently and asynchronously — fully on your own schedule.

Skills

Oncology trials
Trial design
Data analysis
Regulatory standards (FDA EMA)
Scientific feedback
Independent work

Tools

Data annotation tools
AI evaluation workflows
Clinical data analysis software

Job description

Alignerr is seeking an experienced Oncology Clinical Researcher to shape how AI understands oncology by grounding models in real-world clinical trial science. You will review and improve AI-generated oncology content, ensuring regulatory-aligned, scientifically valid outputs.

You’ll work remotely on an hourly contract, 10–40 hours per week, with flexible scheduling. This role suits professionals who want meaningful, independent work and potential ongoing projects with leading AI research teams.

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